DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
SANDOSTATIN LAR
FDA Application No:
(NDA) 021008
Active Ingredient(s):
OCTREOTIDE ACETATE
Company:
NOVARTIS
Original Approval or Tentative Approval Date:
November 25, 1998
Chemical Type:
3 New dosage form
Review Classification:
P Priority review drug
O Orphan drug
There are no Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
SANDOSTATIN LAR
OCTREOTIDE ACETATE
EQ 10MG BASE/VIAL
INJECTABLE; INJECTION
Prescription
No
None
SANDOSTATIN LAR
OCTREOTIDE ACETATE
EQ 20MG BASE/VIAL
INJECTABLE; INJECTION
Prescription
No
None
SANDOSTATIN LAR
OCTREOTIDE ACETATE
EQ 30MG BASE/VIAL
INJECTABLE; INJECTION
Prescription
Yes
None
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